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BMC Medical Genomics

【机译】：BmC医学基因组学

ISSN：-
出版周期：
语言：English

起始发布年份：2008
出版者：London : BioMed Central
出版地：England

NLM刊名缩写：BMC Med Genomics

数据库引入：PubMed: v1 (2008)-, PMC

MeSH词表主题词：Genetics, Medical; Genomics*

备注：Description based on first issue; title from journal home page (publisher's Web展开▼

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1.Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci

机译：使用有限的基因型数据或不使用基因型数据消除参考作图偏倚可鉴定疾病相关位点蛋白质结合的等位基因差异
- 作者：Martin L. Buchkovich;Karl Eklund;Qing Duan;Yun Li;Karen L. Mohlke;Terrence S. Furey
- 期刊名称：《BMC Medical Genomics》 | 2015年第-1期
- Allelic imbalance Genome mapping bias Transcription factor binding CREB1 Inflammatory bowel disease Alleles GWAS ChIP-seq;
2.TumorTracer: a method to identify the tissue of origin from the somatic mutations of a tumor specimen

机译：TumorTracer：一种从肿瘤标本的体细胞突变中识别起源组织的方法
- 作者：Andrea Marion Marquard;Nicolai Juul Birkbak;Cecilia Engel Thomas;Francesco Favero;Marcin Krzystanek;Celine Lefebvre;Charles Ferté;Mariam Jamal-Hanjani;Gareth A. Wilson;Seema Shafi;Charles Swanton;Fabrice André;Zoltan Szallasi;Aron Charles Eklund
- 期刊名称：《BMC Medical Genomics》 | 2015年第-1期
- Cancer of unknown primary Cancer genomics Mutations;
3.Scalable and cost-effective NGS genotyping in the cloud

机译：云中可扩展且经济高效的NGS基因分型
- 作者：Yassine Souilmi;Alex K. Lancaster;Jae-Yoon Jung;Ettore Rizzo;Jared B. Hawkins;Ryan Powles;Saaïd Amzazi;Hassan Ghazal;Peter J. Tonellato;Dennis P. Wall
- 期刊名称：《BMC Medical Genomics》 | 2015年第-1期
- Next-generation sequencing Clinical sequencing Cloud computing Medical genomics Software Bioinformatics Parallel computing;
4.Integrating heterogeneous genomic data to accurately identify disease subtypes

机译：整合异构基因组数据以准确识别疾病亚型
- 作者：Xianwen Ren;Hua Fu;Qi Jin
- 期刊名称：《BMC Medical Genomics》 | 2015年第-1期
- DNA methylation Gene expression miRNA expression Integration Diagnosis Prognosis Cancer stratification;
5.Visualization of genetic disease-phenotype similarities by multiple maps t-SNE with Laplacian regularization

机译：通过多图t-SNE和拉普拉斯正则化可视化遗传疾病-表型的相似性
- 作者：Weiwei Xu;Xingpeng Jiang;Xiaohua Hu;Guangrong Li
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 2期
6.Identifying disease genes by integrating multiple data sources

机译：通过整合多个数据源识别疾病基因
- 作者：Bolin Chen;Jianxin Wang;Min Li;Fang-Xiang Wu
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 2期
- disease gene data integration Markov random field Bayesian analysis;
7.Integrating PPI datasets with the PPI data from biomedical literature for protein complex detection

机译：将PPI数据集与生物医学文献中的PPI数据相集成以进行蛋白质复合物检测
- 作者：Zhi Hao Yang;Feng Ying Yu;Hong Fei Lin;Jian Wang
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 2期
- Protein-protein interaction network Protein complexes Information extraction Text mining;
8.Prediction of disease-related genes based on weighted tissue-specific networks by using DNA methylation

机译：使用DNA甲基化基于加权组织特异性网络预测疾病相关基因
- 作者：Min Li;Jiayi Zhang;Qing Liu;Jianxin Wang;Fang-Xiang Wu
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 2期
9.Supervised redundant feature detection for tumor classification

机译：监督冗余特征检测以进行肿瘤分类
- 作者：Xue-Qiang Zeng;Guo-Zheng Li
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 2期
- Feature selection Redundant feature Microarray data Tumor classification;
10.New horizons in translational bioinformatics: TBC 2013

机译：翻译生物信息学的新视野：TBC 2013
- 作者：Ju Han Kim
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
11.Concordance of deregulated mechanisms unveiled in underpowered experiments: PTBP1 knockdown case study

机译：在动力不足的实验中揭示了放松调节机制的一致性：PTBP1敲低案例研究
- 作者：Vincent Gardeux;Ahmet D Arslan;Ikbel Achour;Tsui-Ting Ho;William T Beck;Yves A Lussier
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
12.In Silico cancer cell versus stroma cellularity index computed from species-specific human and mouse transcriptome of xenograft models: towards accurate stroma targeting therapy assessment

机译：根据异种移植模型的物种特异性人类和小鼠转录组计算出的硅癌细胞与基质细胞流动性指数：朝着准确的基质靶向治疗评估
- 作者：Xinan Yang;Yong Huang;Younghee Lee;Vincent Gardeux;Ikbel Achour;Kelly Regan;Ellen Rebman;Haiquan Li;Yves A Lussier
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
13.Integrative analysis reveals disease-associated genes and biomarkers for prostate cancer progression

机译：整合分析揭示了与疾病相关的基因和前列腺癌进展的生物标志物
- 作者：Yin Li;Wanwipa Vongsangnak;Luonan Chen;Bairong Shen
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
- Biomarker Disease-associated Genes Integrative analysis Prostate cancer Transcription factor;
14.A coupling approach of a predictor and a descriptor for breast cancer prognosis

机译：乳腺癌预后与预测指标的耦合方法
- 作者：Hyunjung Shin;Yonghyun Nam
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
15.Derivative component analysis for mass spectral serum proteomic profiles

机译：质谱分析血清蛋白质组学特征的导数成分分析
- 作者：Henry Han
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
16.IGENT: efficient entropy based algorithm for genome-wide gene-gene interaction analysis

机译：IGENT：用于全基因组全基因-基因相互作用分析的基于熵的高效算法
- 作者：Min-Seok Kwon;Mira Park;Taesung Park
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
17.Predicting phenotypes of asthma and eczema with machine learning

机译：通过机器学习预测哮喘和湿疹的表型
- 作者：Mattia CF Prosperi;Susana Marinho;Angela Simpson;Adnan Custovic;Iain E Buchan
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
- Asthma wheeze eczema allergen lung function single nucleotide polymorphisms machine learning model selection diagnostics;
18.Identification of novel therapeutics for complex diseases from genome-wide association data

机译：从全基因组关联数据中识别复杂疾病的新疗法
- 作者：Mani P Grover;Sara Ballouz;Kaavya A Mohanasundaram;Richard A George;Craig D H Sherman;Tamsyn M Crowley;Merridee A Wouters
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
- Complex disease Candidate gene Drug database Drug target Drug repositioning Genome-wide association study;
19.GAMUT: GPU accelerated microRNA analysis to uncover target genes through CUDA-miRanda

机译：GAMUT：GPU加速的microRNA分析通过CUDA-miRanda发现靶基因
- 作者：Shuang Wang;Jihoon Kim;Xiaoqian Jiang;Stefan F Brunner;Lucila Ohno-Machado
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
20.Integrated analysis of microRNA-target interactions with clinical outcomes for cancers

机译：microRNA-靶标相互作用与癌症临床结果的综合分析
- 作者：Je-Gun Joung;Dokyoon Kim;Su Yeon Lee;Hwa Jung Kang;Ju Han Kim
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
- Survival Analysis miRNA-mRNA interaction miRNA Expression Gene Expression Profile Cancer Genes;
21.Effectively processing medical term queries on the UMLS Metathesaurus by layered dynamic programming

机译：通过分层动态编程有效地处理UMLS词库上的医学术语查询
- 作者：Kaiyu Ren;Albert M Lai;Aveek Mukhopadhyay;Raghu Machiraju;Kun Huang;Yang Xiang
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
22.Automatic detection and resolution of measurement-unit conflicts in aggregated data

机译：自动检测和解决聚合数据中的度量单位冲突
- 作者：Soroush Samadian;Bruce McManus;Mark Wilkinson
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
23.Comparison of warfarin therapy clinical outcomes following implementation of an automated mobile phone-based critical laboratory value text alert system

机译：实施基于自动手机的关键实验室价值文本警报系统后华法林疗法的临床结果比较
- 作者：Shu-Wen Lin;Wen-Yi Kang;Dong-Tsamn Lin;James Chao-Shen Lee;Fe-Lin Lin Wu;Chuen-Liang Chen;Yufeng J Tseng
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
24.Differentially private distributed logistic regression using private and public data

机译：使用私有和公共数据的差分私有分布式逻辑回归
- 作者：Zhanglong Ji;Xiaoqian Jiang;Shuang Wang;Li Xiong;Lucila Ohno-Machado
- 期刊名称：《BMC Medical Genomics》 | 2014年第Suppl 1期
25.The Anatomy to Genomics (ATG) Start Genetics medical school initiative: incorporating exome sequencing data from cadavers used for Anatomy instruction into the first year curriculum

机译：解剖学向基因组学（ATG）启动遗传学医学院倡议：将用于解剖学教学的尸体的外显子组测序数据纳入第一年课程
- 作者：Glenn S. Gerhard;Qunyan Jin;Barbara V. Paynton;Steven N. Popoff
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Exome sequencing Medical education Cadaver;
26.Building towards precision medicine: empowering medical professionals for the next revolution

机译：迈向精密医学：赋予医学专业人士下一次革命的力量
- 作者：Scott McGrath;Dario Ghersi
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
27.Explorations to improve the completeness of exome sequencing

机译：探索提高外显子组测序的完整性
- 作者：Chen Du;Barbara N. Pusey;Christopher J. Adams;C. Christopher Lau;William P. Bone;William A. Gahl;Thomas C. Markello;David R. Adams
- 期刊名称：《BMC Medical Genomics》 | 2016年第1期
- Clinical exome sequencing Analytical quality Performance enhancement Clinical genomics Rare diseases Completeness problem False negative results;
28.Known unknowns: building an ethics of uncertainty into genomic medicine

机译：已知的未知数：将不确定性伦理学纳入基因组医学
- 作者：Ainsley J. Newson;Samantha J. Leonard;Alison Hall;Clara L. Gaff
- 期刊名称：《BMC Medical Genomics》 | 2016年第1期
- Ethics Uncertainty Genomics Clinical genomics Massively parallel sequencing Genome sequencing Genomic testing Genetic counseling Rare diseases Variants of uncertain significance;
29.The IGNITE network: a model for genomic medicine implementation and research

机译：IGNITE网络：基因组医学实施和研究的模型
- 作者：Kristin Wiisanen Weitzel;Madeline Alexander;Barbara A. Bernhardt;Neil Calman;David J. Carey;Larisa H. Cavallari;Julie R. Field;Diane Hauser;Heather A. Junkins;Phillip A. Levin;Kenneth Levy;Ebony B. Madden;Teri A. Manolio;Jacqueline Odgis;Lori A. Orlando;Reed Pyeritz;R. Ryanne Wu;Alan R. Shuldiner;Erwin P. Bottinger;Joshua C. Denny;Paul R. Dexter;David A. Flockhart;Carol R. Horowitz;Julie A. Johnson;Stephen E. Kimmel;Mia A. Levy;Toni I. Pollin;Geoffrey S. Ginsburg
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Precision medicine Pharmacogenomics Genomics Personalized medicine Clinical decision support Electronic health record Implementation;
30.Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

机译：中国汉族人群先天性室间隔缺损的全基因组拷贝数变异分析
- 作者：Yu An;Wenyuan Duan;Guoying Huang;Xiaoli Chen;Li Li;Chenxia Nie;Jia Hou;Yonghao Gui;Yiming Wu;Feng Zhang;Yiping Shen;Bailin Wu;Hongyan Wang
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Ventricular septal defect aCGH Congenital heart defect Copy number variants;
31.A comparison of genomic profiles of complex diseases under different models

机译：不同模型下复杂疾病基因组谱的比较
- 作者：Víctor Potenciano;María Mar Abad-Grau;Antonio Alcina;Fuencisla Matesanz
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
32.SFRP1 is a possible candidate for epigenetic therapy in non-small cell lung cancer

机译：SFRP1在非小细胞肺癌中可能是表观遗传学治疗的候选药物
- 作者：Y-h. Taguchi;Mitsuo Iwadate;Hideaki Umeyama
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
33.Machine learning derived risk prediction of anorexia nervosa

机译：机器学习得出神经性厌食症的风险预测
- 作者：Yiran Guo;Zhi Wei;Brendan J. Keating;Hakon Hakonarson
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Anorexia nervosa Machine learning Genome wide association Risk prediction Genotyping;
34.Discovering gene expression signatures responding to tyrosine kinase inhibitor treatment in chronic myeloid leukemia

机译：发现酪氨酸激酶抑制剂治疗慢性粒细胞白血病的基因表达特征
- 作者：Kihoon Cha;Yi Li;Gwan-Su Yi
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- Gene expression signature Chronic myeloid leukemia (CML) Tyrosine kinase inhibitor (TKI) Meta-analysis Random forest;
35.Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes protein folding pathways and GWAS loci in Parkinson disease

机译：蛋白质组学和RNA转录组学的综合分析涉及帕金森病的线粒体过程蛋白质折叠途径和GWAS基因座
- 作者：Alexandra Dumitriu;Javad Golji;Adam T. Labadorf;Benbo Gao;Thomas G. Beach;Richard H. Myers;Kenneth A. Longo;Jeanne C. Latourelle
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Parkinson disease RNA-Seq MS3 proteomics GWAS loci Data integration Metallothioneins Mitochondria Protein folding pathways;
36.Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer’s disease

机译：整合生物信息学和影像学信息学以鉴定阿尔茨海默氏病中罕见的PSEN1变异
- 作者：Kwangsik Nho;Emrin Horgusluoglu;Sungeun Kim;Shannon L. Risacher;Dokyoon Kim;Tatiana Foroud;Paul S. Aisen;Ronald C. Petersen;Clifford R. Jack Jr.;Leslie M. Shaw;John Q. Trojanowski;Michael W. Weiner;Robert C. Green;Arthur W. Toga;Andrew J. Saykin
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- Whole genome sequencing Imaging genetics Gene-based association of rare variants PSEN1;
37.Gene expression profiling in necrotizing enterocolitis reveals pathways common to those reported in Crohn’s disease

机译：坏死性小肠结肠炎的基因表达谱揭示了克罗恩病报道的常见途径
- 作者：Éric Tremblay;Marie-Pier Thibault;Emanuela Ferretti;Corentin Babakissa;Valérie Bertelle;Marcos Bettolli;Karolina Maria Burghardt;Jean-François Colombani;David Grynspan;Emile Levy;Peng Lu;Sandeep Mayer;Daniel Ménard;Olivier Mouterde;Ingrid B. Renes;Ernest G. Seidman;Jean-François Beaulieu
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Human intestine Preterm birth Transcriptomics Gene expression Immune response;
38.Integrative regression network for genomic association study

机译：整合回归网络进行基因组关联研究
- 作者：Reddy Rani Vangimalla;Hyun-hwan Jeong;Kyung-Ah Sohn
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- Genomic association Sparse regression Similarity fusion network Integrative analysis TCGA;
39.Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly

机译：全外显子测序是在智力障碍和小头畸形患者中进行病因诊断的有效方法
- 作者：Patrick Rump;Omid Jazayeri;Krista K. van Dijk-Bos;Lennart F. Johansson;Anthonie J. van Essen;Johanna B. G. M. Verheij;Hermine E. Veenstra-Knol;Egbert J. W. Redeker;Marcel M. A. M. Mannens;Morris A. Swertz;Behrooz Z. Alizadeh;Conny M. A. van Ravenswaaij-Arts;Richard J. Sinke;Birgit Sikkema-Raddatz
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Autosomal recessive inheritance ASPM BRCA2 CASK DYRK1A ERCC8 KIF11 Microcephaly RAB3GAP1 RNASEH2B RTTN Whole-exome sequencing;
40.eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

机译：eMERGE现象广泛关联研究（PheWAS）确定了终止增益变异的临床关联和多效性
- 作者：Anurag Verma;Shefali S. Verma;Sarah A. Pendergrass;Dana C. Crawford;David R. Crosslin;Helena Kuivaniemi;William S. Bush;Yuki Bradford;Iftikhar Kullo;Suzette J. Bielinski;Rongling Li;Joshua C. Denny;Peggy Peissig;Scott Hebbring;Mariza De Andrade;Marylyn D. Ritchie;Gerard Tromp
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
41.Differential gene network analysis for the identification of asthma-associated therapeutic targets in allergen-specific T-helper memory responses

机译：差异基因网络分析用于鉴定与哮喘相关的治疗靶标的变应原特异性T辅助记忆反应
- 作者：Niamh M. Troy;Elysia M. Hollams;Patrick G. Holt;Anthony Bosco
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Asthma Atopy House dust mite Microarray Raine study CD4 T cell Differential network analysis;
42.Integrated analysis of omics data using microRNA-target mRNA network and PPI network reveals regulation of Gnai1 function in the spinal cord of Ews/Ewsr1 KO mice

机译：使用microRNA靶mRNA网络和PPI网络对组学数据进行的综合分析揭示了Ews / Ewsr1 KO小鼠脊髓中Gnai1功能的调节
- 作者：Chai-Jin Lee;Hongryul Ahn;Sean Bong Lee;Jong-Yeon Shin;Woong-Yang Park;Jong-Il Kim;Junghee Lee;Hoon Ryu;Sun Kim
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- EWS Ewsr1 Gnai1 MMIA PPI Network analysis;
43.SOX5 is involved in balanced MITF regulation in human melanoma cells

机译：SOX5参与人黑素瘤细胞中MITF的平衡调节
- 作者：Theresa Kordaß;Claudia E. M. Weber;Marcus Oswald;Volker Ast;Mathias Bernhardt;Daniel Novak;Jochen Utikal;Stefan B. Eichmüller;Rainer König
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- SOX5 MITF SOX10 Melanoma Mixed Integer Linear Programming Regulatory models;
44.Inferring Crohn’s disease association from exome sequences by integrating biological knowledge

机译：通过整合生物学知识从外显子组序列推断克罗恩病关联
- 作者：Chan-Seok Jeong;Dongsup Kim
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
45.Cancer survival analysis using semi-supervised learning method based on Cox and AFT models with L1/2 regularization

机译：基于Cox和AFT模型并采用L1 / 2正则化的半监督学习方法进行癌症生存分析
- 作者：Yong Liang;Hua Chai;Xiao-Ying Liu;Zong-Ben Xu;Hai Zhang;Kwong-Sak Leung
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Cancer survival analysis Semi-supervised learning Gene selection Regularization Cox proportional hazards model Accelerated failure time model;
46.Fast comparison of genomic and meta-genomic reads with alignment-free measures based on quality values

机译：通过基于质量值的无比对措施快速比较基因组和元基因组读数
- 作者：Matteo Comin;Michele Schimd
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- Meta-genomes Phylogeny without assembly Alignment-free measures Reads quality values;
47.Efficient and biologically relevant consensus strategy for Parkinson’s disease gene prioritization

机译：帕金森氏病基因优先排序的有效且生物学相关的共识策略
- 作者：Maykel Cruz-Monteagudo;Fernanda Borges;Cesar Paz-y-Miño;M. Natália D. S. Cordeiro;Irene Rebelo;Yunierkis Perez-Castillo;Aliuska Morales Helguera;Aminael Sánchez-Rodríguez;Eduardo Tejera
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Consensus strategy Co-expression networks Early recognition Gene prioritization Parkinson’s disease;
48.Major methylation alterations on the CpG markers of inflammatory immune associated genes after IVIG treatment in Kawasaki disease

机译：川崎病IVIG治疗后炎症免疫相关基因CpG标记的主要甲基化改变
- 作者：Sung-Chou Li;Wen-Ching Chan;Ying-Hsien Huang;Mindy Ming-Huey Guo;Hong-Ren Yu;Fu-Chen Huang;Hsing-Chun Kuo;Ho-Chang Kuo
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- Kawasaki disease DNA methylation CpG marker Intravenous immunoglobulin Methylation alteration;
49.Transcriptome analysis reveals a ribosome constituents disorder involved in the RPL5 downregulated zebrafish model of Diamond-Blackfan anemia

机译：转录组分析揭示了与RPL5下调的Diamond-Blackfan贫血斑马鱼模型有关的核糖体成分疾病
- 作者：Yang Wan;Qian Zhang;Zhaojun Zhang;Binfeng Song;Xiaomin Wang;Yingchi Zhang;Qiong Jia;Tao Cheng;Xiaofan Zhu;Anskar Yu-Hung Leung;Weiping Yuan;Haibo Jia;Xiangdong Fang
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- DBA RPL5 RNA-seq ncRNA-seq Zebrafish;
50.Frequent hypermethylation of orphan CpG islands with enhancer activity in cancer

机译：孤儿CpG岛频繁甲基化并具有增强剂活性
- 作者：Min Gyun Bae;Jeong Yeon Kim;Jung Kyoon Choi
- 期刊名称：《BMC Medical Genomics》 | 2016年第Suppl 1期
- CpG islands Enhancers DNA methylation Cancer;
51.Experiences and attitudes of residents regarding a community-based genome cohort study in Japan: a population-based cross-sectional study

机译：日本居民基于社区的基因组队列研究的经验和态度：基于人群的横断面研究
- 作者：Keiko Miyamoto;Miho Iwakuma;Takeo Nakayama
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Public attitude Genome study Drug susceptibility Familiarity Japan;
52.Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma

机译：小梁网中的遗传关联和压力介导的下调暗示MPP7是原发性开角型青光眼的新候选基因
- 作者：Mansi Vishal;Anchal Sharma;Lalit Kaurani;Giovanna Alfano;Suddhasil Mookherjee;Kiran Narta;Jyoti Agrawal;Iman Bhattacharya;Susanta Roychoudhury;Jharna Ray;Naushin H. Waseem;Shomi S. Bhattacharya;Analabha Basu;Abhijit Sen;Kunal Ray;Arijit Mukhopadhyay
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- POAG IOP MPP7 GWA HTM LD GEO SNP;
53.Case-oriented pathways analysis in pancreatic adenocarcinoma using data from a sleeping beauty transposon mutagenesis screen

机译：利用沉睡的美容转座子诱变筛查数据分析胰腺腺癌的病例导向途径
- 作者：Yen-Yi Ho;Timothy K. Starr;Rebecca S. LaRue;David A. Largaespada
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Forward genetic screen Sleeping Beauty transposon Case-oriented gene set analysis Pathways correlations CIS Common insertion sites;
54.Saliva DNA quality and genotyping efficiency in a predominantly elderly population

机译：老年人群中唾液DNA的质量和基因分型效率
- 作者：Harini V. Gudiseva;Mark Hansen;Linda Gutierrez;David W. Collins;Jie He;Lana D. Verkuil;Ian D. Danford;Anna Sagaser;Anita S. Bowman;Rebecca Salowe;Prithvi S. Sankar;Eydie Miller-Ellis;Amanda Lehman;Joan M. O’Brien
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Saliva Blood DNA Genotyping Microarrays GWAS SNPs Elderly Glaucoma African-Americans 260/280 absorbance Call rates;
55.A microRNA biomarker of hepatocellular carcinoma recurrence following liver transplantation accounting for within-patient heterogeneity

机译：肝移植后肝细胞癌复发的microRNA生物标志物说明了患者内的异质性
- 作者：Qing Yan Xie;Anthony Almudevar;Christa L. Whitney-Miller;Christopher T. Barry;Matthew N. McCall
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- microRNA Biomarker Hepatocellular carcinoma (HCC) Liver transplantation Recurrence;
56.Longitudinal genome-wide methylation study of Roux-en-Y gastric bypass patients reveals novel CpG sites associated with essential hypertension

机译：Roux-en-Y胃旁路患者的纵向全基因组甲基化研究揭示了与原发性高血压相关的新CpG位点
- 作者：Adrian E. Boström;Jessica Mwinyi;Sarah Voisin;Wenting Wu;Bernd Schultes;Kang Zhang;Helgi B. Schiöth
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Essential hypertension Epigenome-wide association study Whole methylome analysis Bariatric surgery EHMT2 FUSSEL18 SKOR2 Corl2;
57.Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based case-control study

机译：microRNA生物发生基因中的多态性对结肠癌风险和microRNA表达水平的影响：基于人群的病例对照研究
- 作者：Lila E. Mullany;Jennifer S. Herrick;Roger K. Wolff;Matthew F. Buas;Martha L. Slattery
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- miRNA Biogenesis SNP Colon Cancer Risk;
58.Comparison of two high-throughput semiconductor chip sequencing platforms in noninvasive prenatal testing for Down syndrome in early pregnancy

机译：两种高通量半导体芯片测序平台在妊娠早期唐氏综合症的无创产前检测中的比较
- 作者：Sunshin Kim;HeeJung Jung;Sung Hee Han;SeungJae Lee;JeongSub Kwon;Min Gyun Kim;Hyungsik Chu;Hongliang Chen;Kyudong Han;Hwanjong Kwak;Sunghoon Park;Hee Jae Joo;Byung Chul Kim;Jong Bhak
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Non-invasive prenatal testing Sequencing Circulating fetal DNA Trisomy Genome;
59.Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing

机译：使用高通量微流控技术和下一代测序技术扩大针对犹太人群的孕前载体筛选
- 作者：Moran Gal;Khen Khermesh;Michal Barak;Min Lin;Hadas Lahat;Haike Reznik Wolf;Michael Lin;Elon Pras;Erez Y. Levanon
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Carrier screening Next generation sequencing Microfluidics Genetic testing Jewish population;
60.Breast cancer subtype predictors revisited: from consensus to concordance?

机译：乳腺癌亚型预测因子：从共识到一致性？
- 作者：Herman MJ. Sontrop;Marcel JT. Reinders;Perry D. Moerland
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Breast cancer Subtype Single sample predictor Concordance Gene expression;
61.Study design and data analysis considerations for the discovery of prognostic molecular biomarkers: a case study of progression free survival in advanced serous ovarian cancer

机译：发现预后分子生物标志物的研究设计和数据分析注意事项：晚期浆液性卵巢癌无进展生存的案例研究
- 作者：Li-Xuan Qin;Douglas A. Levine
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
62.Acute appendicitis: transcript profiling of blood identifies promising biomarkers and potential underlying processes

机译：急性阑尾炎：血液的转录本分析表明有前途的生物标志物和潜在的潜在过程
- 作者：Lakhmir S. Chawla;Ian Toma;Danielle Davison;Khashayar Vaziri;Juliet Lee;Raymond Lucas;Michael G. Seneff;Aoibhinn Nyhan;Timothy A. McCaffrey
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Appendicitis Transcript profiling Biomarkers Interleukin-8 receptor Alkaline phosphatase Defensin;
63.Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

机译：大多数近亲阿拉伯神经病患者的外显子组测序可提供较高的潜在分子诊断率
- 作者：Wu-Lin Charng;Ender Karaca;Zeynep Coban Akdemir;Tomasz Gambin;Mehmed M. Atik;Shen Gu;Jennifer E. Posey;Shalini N. Jhangiani;Donna M. Muzny;Harsha Doddapaneni;Jianhong Hu;Eric Boerwinkle;Richard A. Gibbs;Jill A. Rosenfeld;Hong Cui;Fan Xia;Kandamurugu Manickam;Yaping Yang;Eissa A. Faqeih;Ali Al Asmari;Mohammed A. M. Saleh;Ayman W. El-Hattab;James R. Lupski
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Whole exome sequencing (WES) Copy Number Variants (CNV) Neurodevelopment Developmental Delay/Intellectual Disability (DD/ID) GRM7;
64.Dealing with prognostic signature instability: a strategy illustrated for cardiovascular events in patients with end-stage renal disease

机译：处理预后标志性不稳定：末期肾病患者心血管事件的策略说明
- 作者：Harald Binder;Thorsten Kurz;Sven Teschner;Clemens Kreutz;Marcel Geyer;Johannes Donauer;Annette Kraemer-Guth;Jens Timmer;Martin Schumacher;Gerd Walz
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Prognostic signature Stability Clinical endpoint Outlier;
65.Shared and unique common genetic determinants between pediatric and adult celiac disease

机译：小儿和成人腹腔疾病之间共享且独特的共同遗传决定因素
- 作者：Sabyasachi Senapati;Ajit Sood;Vandana Midha;Neena Sood;Suresh Sharma;Lalit Kumar;B. K. Thelma
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Pediatric celiac disease Adult celiac disease Immunochip HLA-DQ ANK3;
66.A network based approach to drug repositioning identifies plausible candidates for breast cancer and prostate cancer

机译：基于网络的药物重新定位方法可确定乳腺癌和前列腺癌的候选药物
- 作者：Hsiao-Rong Chen;David H. Sherr;Zhenjun Hu;Charles DeLisi
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Computational drug repositioning Drug screening Cancer treatment;
67.Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users’ views

机译：临床全外显子组测序未解决的挑战：对最终用户观点的系统文献综述
- 作者：Gabrielle Bertier;Martin Hétu;Yann Joly
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
68.Reproducible detection of disease-associated markers from gene expression data

机译：从基因表达数据可重复检测疾病相关标记
- 作者：Katsuhiro Omae;Osamu Komori;Shinto Eguchi
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Gene expression analysis Genes screening Heterogeneity Subsampling method Two-sample test U-statistic;
69.Reliable gene expression profiling of formalin-fixed paraffin-embedded breast cancer tissue (FFPE) using cDNA-mediated annealing extension selection and ligation whole-genome (DASL WG) assay

机译：福尔马林固定石蜡包埋的乳腺癌组织（FFPE）的可靠基因表达谱分析采用cDNA介导的退火延伸选择和连接全基因组（DASL WG）分析
- 作者：Mahesh Iddawela;Oscar M. Rueda;Marcus Klarqvist;Stefan Graf;Helena M. Earl;Carlos Caldas
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- FFPE WG DASL Molecular Markers Breast Cancer;
70.Within-pair differences of DNA methylation levels between monozygotic twins are different between male and female pairs

机译：单卵双胞胎之间DNA甲基化水平的配对内差异在男性和女性对之间是不同的
- 作者：Mikio Watanabe;Chika Honda;Yoshinori Iwatani;Shiro Yorifuji;Hiroyasu Iso;Kei Kamide;Jun Hatazawa;Shinji Kihara;Norio Sakai;Hiroko Watanabe;Kiyoko Makimoto;Mikio Watanabe;Chika Honda;Yoshinori Iwatani
- 期刊名称：《BMC Medical Genomics》 | 2016年第1期
- Methylation Monozygotic twin Individual difference Epigenetic change;
71.A 19-Gene expression signature as a predictor of survival in colorectal cancer

机译：19基因表达信号可预测大肠癌生存
- 作者：Nurul Ainin Abdul Aziz;Norfilza M. Mokhtar;Roslan Harun;Md Manir Hossain Mollah;Isa Mohamed Rose;Ismail Sagap;Azmi Mohd Tamil;Wan Zurinah Wan Ngah;Rahman Jamal
- 期刊名称：《BMC Medical Genomics》 | 2016年第1期
- Colorectal cancer Microarray analysis Survivalm Real-time PCR;
72.Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

机译：Immunoseq：通过针对性捕获和测序人类免疫细胞中活性调节区来鉴定功能相关变体
- 作者：Andréanne Morin;Tony Kwan;Bing Ge;Louis Letourneau;Maria Ban;Karolina Tandre;Maxime Caron;Johanna K. Sandling;Jonas Carlsson;Guillaume Bourque;Catherine Laprise;Alexandre Montpetit;Ann-Christine Syvanen;Lars Ronnblom;Stephen J. Sawcer;Mark G. Lathrop;Tomi Pastinen
- 期刊名称：《BMC Medical Genomics》 | 2016年第1期
- Rare variants Immune disease Gene expression Next-generation sequencing Capture;
73.Genome-wide positioning of bivalent mononucleosomes

机译：二价单核小体的全基因组定位
- 作者：Subhojit Sen;Kirsten F. Block;Alice Pasini;Stephen B. Baylin;Hariharan Easwaran
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Bivalent mononucleosomes Bivalency DNA methylation Chromatin H3K4me3 H3K27me3;
74.An adaptive detection method for fetal chromosomal aneuploidy using cell-free DNA from 447 Korean women

机译：利用447名韩国女性的无细胞DNA进行胎儿染色体非整倍性的自适应检测方法
- 作者：Sunshin Kim;HeeJung Jung;Sung Hee Han;SeungJae Lee;JeongSub Kwon;Min Gyun Kim;Hyungsik Chu;Kyudong Han;Hwanjong Kwak;Sunghoon Park;Hee Jae Joo;Minae An;Jungsu Ha;Kyusang Lee;Byung Chul Kim;Hailing Zheng;Xinqiang Zhu;Hongliang Chen;Jong Bhak
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Non-invasive prenatal testing Adaptive detection algorithm Sequencing Circulating fetal DNA Trisomy Genome;
75.Pitfalls of improperly procured adjacent non-neoplastic tissue for somatic mutation analysis using next-generation sequencing

机译：使用下一代测序技术对不正确采购的邻近非肿瘤组织的陷阱进行体细胞突变分析
- 作者：Lei Wei;Antonios Papanicolau-Sengos;Song Liu;Jianmin Wang;Jeffrey M. Conroy;Sean T. Glenn;Elizabeth Brese;Qiang Hu;Kiersten Marie Miles;Blake Burgher;Maochun Qin;Karen Head;Angela R. Omilian;Wiam Bshara;John Krolewski;Donald L. Trump;Candace S. Johnson;Carl D. Morrison
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Somatic mutations Tumor contamination Adjacent normal tissues;
76.A meta-analysis of public microarray data identifies gene regulatory pathways deregulated in peripheral blood mononuclear cells from individuals with Systemic Lupus Erythematosus compared to those without

机译：对公共微阵列数据的荟萃分析确定了与没有系统性红斑狼疮的个体相比外周血单个核细胞中的基因调控通路被解除调节
- 作者：Wendy Kröger;Darlington Mapiye;Jean-Baka Domelevo Entfellner;Nicki Tiffin
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Lupus Systemic Lupus Erythematosus (SLE) Microarray Gene expression Meta-analysis;
77.A rising tide lifts all boats: establishing a multidisciplinary genomic tumor board for breast cancer patients with advanced disease

机译：涨潮掀起了大浪：为患有晚期疾病的乳腺癌患者建立一个多学科的基因组肿瘤委员会
- 作者：Michelle L. McGowan;Roselle S. Ponsaran;Paula Silverman;Lyndsay N. Harris;Patricia A. Marshall
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Breast cancer Genomics Qualitative research Patient care Ethics;
78.DNA methylation patterns associated with oxidative stress in an ageing population

机译：老年人口中与氧化应激相关的DNA甲基化模式
- 作者：Åsa K. Hedman;Mihkel Zilmer;Johan Sundström;Lars Lind;Erik Ingelsson
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- DNA methylation Epigenetics Oxidative stress Type 2 diabetes Cardiovascular disease;
79.Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

机译：先天性胆管扩张的遗传研究确定了功能相关基因的从头和遗传变异
- 作者：John K. L. Wong;Desmond Campbell;Ngoc Diem Ngo;Fanny Yeung;Guo Cheng;Clara S. M. Tang;Patrick H. Y. Chung;Ngoc Son Tran;Man-ting So;Stacey S. Cherny;Pak C. Sham;Paul K. Tam;Maria-Mercè Garcia-Barcelo
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Choledochal cyst Exome De novo Rare variants association;
80.Annual Acknowledgement of Reviewers

机译：年度审稿人致谢
- 作者：Timothy R. Sands
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
81.A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer

机译：对遗传性乳腺癌和卵巢癌意义不确定的非编码变体进行优先级排序的统一分析框架
- 作者：Eliseos J. Mucaki;Natasha G. Caminsky;Ami M. Perri;Ruipeng Lu;Alain Laederach;Matthew Halvorsen;Joan H. M. Knoll;Peter K. Rogan
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Information theory Hereditary breast and ovarian cancer Transcription factor binding RNA-binding protein Prioritization Variants of uncertain significance Splicing Non-coding Next-generation sequencing;
82.Protecting genomic data analytics in the cloud: state of the art and opportunities

机译：保护云中的基因组数据分析：最新技术和机遇
- 作者：Haixu Tang;Xiaoqian Jiang;Xiaofeng Wang;Shuang Wang;Heidi Sofia;Dov Fox;Kristin Lauter;Bradley Malin;Amalio Telenti;Li Xiong;Lucila Ohno-Machado
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
83.Adaptation of a RAS pathway activation signature from FF to FFPE tissues in colorectal cancer

机译：大肠癌中从FF到FFPE组织的RAS途径激活信号的适应性
- 作者：Bernard Omolo;Mingli Yang;Fang Yin Lo;Michael J. Schell;Sharon Austin;Kellie Howard;Anup Madan;Timothy J. Yeatman
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
- Colorectal cancer FF (fresh-frozen) FFPE (formalin-fixed Paraffin embedded) Microarray NanoString RAS pathway signature RNASeq;
84.Erratum to: RNA sequencing reveals a depletion of collagen targeting microRNAs in Dupuytren’s disease

机译：勘误到：RNA测序揭示了Dupuytren病中胶原靶向microRNA的消耗
- 作者：Scott M. Riester;Diren Arsoy;Emily T. Camilleri;Amel Dudakovic;Christopher R. Paradise;Jared M. Evans;Jorge Torres-Mora;Marco Rizzo;Peter Kloen;Marianna Kruithof-de Julio;Andre J. van Wijnen;Sanjeev Kakar
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
85.Erratum to: Breast cancer subtype predictors revisited: from consensus to concordance?

机译：勘误表：乳腺癌亚型预测因子：从共识到一致？
- 作者：Herman M. J. Sontrop;Marcel J. T. Reinders;Perry D. Moerland
- 期刊名称：《BMC Medical Genomics》 | 2016年第-1期
86.Konnector v2.0: pseudo-long reads from paired-end sequencing data

机译：Konnector v2.0：从配对末端测序数据中进行伪长读取
- 作者：Benjamin P Vandervalk;Chen Yang;Zhuyi Xue;Karthika Raghavan;Justin Chu;Hamid Mohamadi;Shaun D Jackman;Readman Chiu;René L Warren;Inanç Birol
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 3期
- Bloom filter de Bruijn graph paired-end sequencing de novo genome assembly;
87.A fast and high performance multiple data integration algorithm for identifying human disease genes

机译：用于识别人类疾病基因的快速高性能的多数据集成算法
- 作者：Bolin Chen;Min Li;Jianxin Wang;Xuequn Shang;Fang-Xiang Wu
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 3期
- disease gene Bayesian analysis logistic regression multiple data integration feature vector;
88.Refining multivariate disease phenotypes for high chip heritability

机译：完善多变量疾病表型提高芯片遗传力
- 作者：Jiangwen Sun;Henry R Kranzler;Jinbo Bi
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 3期
- phenotype-genotype association analysis chip heritability quadratic optimization heritable component analysis;
89.Patient classification of hypertension in Traditional Chinese Medicine using multi-label learning techniques

机译：使用多标签学习技术对中医高血压患者进行分类
- 作者：Guo-Zheng Li;Zehui He;Feng-Feng Shao;Ai-Hua Ou;Xiao-Zhong Lin
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 3期
- Traditional Chinese medicine Multi-label learning Data mining Feature selection;
90.Hybrid de novo tandem repeat detection using short and long reads

机译：使用短读和长读的混合从头串联重复检测
- 作者：Guillaume Fertin;Géraldine Jean;Andreea Radulescu;Irena Rusu
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 3期
- tandem repeat second-generation sequencing third-generation sequencing de Bruijn graph;
91.A computational method for identification of vaccine targets from protein regions of conserved human leukocyte antigen binding

机译：一种从保守的人白细胞抗原结合蛋白区域识别疫苗靶标的计算方法
- 作者：Lars R Olsen;Christian Simon;Ulrich J Kudahl;Frederik O Bagger;Ole Winther;Ellis L Reinherz;Guang L Zhang;Vladimir Brusic
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 4期
- bioinformatics T cell immunity epitope prediction conservation analysis cross-reactivity;
92.LENS: web-based lens for enrichment and network studies of human proteins

机译：镜头：基于网络的镜头用于人类蛋白质的富集和网络研究
- 作者：Adam Handen;Madhavi K Ganapthiraju
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 4期
93.Prediction of linear B-cell epitopes of hepatitis C virus for vaccine development

机译：丙型肝炎病毒线性B细胞表位的预测用于疫苗开发
- 作者：Wen-Lin Huang;Ming-Ju Tsai;Kai-Ti Hsu;Jyun-Rong Wang;Yi-Hsiung Chen;Shinn-Ying Ho
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 4期
94.g-FLUA2H: a web-based application to study the dynamics of animal-to-human mutation transmission for influenza viruses

机译：g-FLUA2H：基于Web的应用程序用于研究流感病毒从动物到人的突变传播的动力学
- 作者：Muhammad Farhan Sjaugi;Swan Tan;Hadia Syahirah Abd Raman;Wan Ching Lim;Nik Elena Nik Mohamed;J Thomas August;Asif M Khan
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 4期
- influenza viruses animal-to-human transmission mutation;
95.A systematic analysis of a broadly neutralizing antibody AR3C epitopes on Hepatitis C virus E2 envelope glycoprotein and their cross-reactivity

机译：丙型肝炎病毒E2包膜糖蛋白上广泛中和的抗体AR3C表位的系统分析及其交叉反应性
- 作者：Jing Sun;Vladimir Brusic
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 4期
96.Connecting the dots in translational bioinformatics: TBC 2014 collection

机译：连接翻译生物信息学中的点点滴滴：TBC 2014系列
- 作者：Ju Han Kim
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 2期
97.Novel therapeutics for coronary artery disease from genome-wide association study data

机译：来自全基因组关联研究数据的冠状动脉疾病的新疗法
- 作者：Mani P Grover;Sara Ballouz;Kaavya A Mohanasundaram;Richard A George;Andrzej Goscinski;Tamsyn M Crowley;Craig D H Sherman;Merridee A Wouters
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 2期
- Coronary Artery Disease Genome-wide association study Candidate gene Drug database Drug target Drug repositioning;
98.Inferring drug-disease associations based on known protein complexes

机译：基于已知蛋白复合物推断药物-疾病关联
- 作者：Liang Yu;Jianbin Huang;Zhixin Ma;Jing Zhang;Yapeng Zou;Lin Gao
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 2期
- Drug-disease associations protein complexes drug repositioning weighted network;
99.Interpretation of personal genome sequencing data in terms of disease ranks based on mutual information

机译：根据互助信息按疾病等级解释个人基因组测序数据
- 作者：Young-Ji Na;Kyung-Ah Sohn;Ju Han Kim
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 2期
- Next-generation sequencing MeSH tree structure disease risk personal genome;
100.Identification of epigenetic modifications that contribute to pathogenesis in therapy-related AML: Effective integration of genome-wide histone modification with transcriptional profiles

机译：鉴定有助于治疗相关AML发病机理的表观遗传修饰：将全基因组组蛋白修饰与转录谱有效整合
- 作者：Xinan (Holly) Yang;Bin Wang;John M Cunningham
- 期刊名称：《BMC Medical Genomics》 | 2015年第Suppl 2期
- computational biology t-AML EZH2 H3K27me3 SEMA3A;